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by Sherilyn Go to last post
113 212,248
i had ETS on Weds. Insurance covered most of the cost. Out of pocket to me was a little more than $2,000. First two days were painful. Difficulty breathing, etc but pain meds helped cope. Just this evening, noticed both hands getting sweaty again, albeit slightly.. I have read that this happens in some cases and is temporary. I will post... by TxGuy
by TxGuy Go to last post
39 7,969
Hi, This is a bit of a long shot but does anyone in the UK have a weeks worth of avert/robinul I could buy off them? I suffer badly from HH and due to go to on holiday this Sunday. Ive placed an order but it hasn't arrived yet and I've ran out of it. As you can imagine, I'm in a bit of a desperate situation right now so any help would be... by harry374
by driping jon Go to last post
3 997
I have generalized hyperhydrosis. Are there any treatments which can treat the full body? I am on oxybutin which works somewhat but is not consistent and the side effects can be horrible. I live in the tropics and so in the summer 10-20mg of oxybutin, I can still sweat bullets all over. Subcut glycopylorate works great but my GP doesn't want me... by GM79
by Sprawling Go to last post
1 826
Hey everyone, was just wondering if anyone had any experience or insight into using pilocarpine to help mediate some of the dry mouth/dry eyes caused by oxybuytnin. I've tried oxybutynin before and went up to 10mg and noticed a moderate reduction in my palmar plantar hyperhidrosis but the dry mouth and brain fog was just too much. I've... by jamessmith112
by SerSweatsalot Go to last post
2 1,284
Has anyone tried this? It's an anticholinergic similar to Glycopyrrolate or Oxybutynin but with less dry mouth. by SerSweatsalot
by SerSweatsalot Go to last post
4 873
hi.has anyone had problems getting hold of pro-banthine.there looks to be a issue with this from where i usually buy it.i have been trying to get some for a few months now by driping jon
by driping jon Go to last post
5 1,117
Hi All, Came across the website above by chance. The author is Miles Dawson. Selling a system for only $37. Scam or legit? Anyone try yet? TIA! Cheers, by Z33
by Sprawling Go to last post
1 773
Brothers of the same pain HH, i greet you all especially our most contributing Friend Sprawling :greeting: Months after months lurking and reading nearly all post, i have finally joined this site to help my self in the fight against HH, reading Sprawling post has really helped me alot in terms of ionto devices used and such, so thanks... by Jadal
by Sprawling Go to last post
7 968
Brenda posted about this product and I figured it should have its own topic: Here's an interesting product that I had no idea existed. It seems to be available in the United States as an "Oxybutynin topical" Gelnique. Sounds like this can be a good alternative to "secure wipes" from in Canada. I don't think it's over the... by Sprawling
by Sprawling Go to last post
2 1,200
Hi there I've been seeing a dermatologist for hiperhidrosis for a few years now. Tried everything: oxybutynin, beta blockers, glycopyrolate, iontophoresis... the only thing that worked on my hands is botox! Anyway... I've been offered no solution for the lower back/crotch area. I have a feeling there may be an underlying condition or... by laurenzo
by Sprawling Go to last post
12 2,022
Hi people! I'm new here as you see, and with the same problem as you: HH. It's my first time trying Iontophoresis, as I can't afford a machine I've made a homemade intophoresis machine with two 9V batteries which are 8.4V indeed, because they're rechargeable ones. Also two aluminum food trails to conduct electricity. This is my eighth day with no... by sweatless
by Sprawling Go to last post
16 2,097
When I first began my iontophoresis treatment for my hands I used just enough water to submerge my hands but my finger tips were always still sweaty because the water did not reach it. After two or three weeks I stopped sweating, but my finger tips did not and that did not bother me too much because it was a small surface area. I eventually... by navpal
by Sprawling Go to last post
2 809
Hi everybody, My name is Mike and i have suffered from facial hyperhidrosis for the last few years (26 years old) It realy had and still have effected on my whole life, and of course influeneced on my confidence and mood. I have tried sweat block something like a week ago, and its realy changed my life, at least until now. I really dont... by MikeAS
by Sprawling Go to last post
5 878
Is iontophoresis more effective above 25mA and is there any way to configure an idromed 5 PS to increase the current output? by BaconOnline
by Sprawling Go to last post
1 668
Hi there, just trying to see if there is anyone in London who would like to meet at some point. I am 44 and kind of have accepted that I will have hyperhidrosis for my whole life but is still puzzling to me that I never came across anyone with this condition. If in London, hope you are all doing well with those hot days! All the best Vasia by vas171
by Sprawling Go to last post
2 775
Hi All, I'm at a point where I need some extra help with Axillary HH, I've tried a lot of things below: Antiperspirants: like Certraindri, Sweatblock and a few others that are not even allowed in the US, they worked for a bit but now they stopped working. I had botox injections which worked great for about 6 months, then I had a second... by msbustillo
by msbustillo Go to last post
1 807
This will be pretty much identical to posts on other forums that I have made, but I just wanted to make sure it made it here to reach everyone. I am currently in contact with the international hyperhidrosis society in regards to ways to raise awareness and call for more research into this horrible condition. So far I have created a petition... by juanes_piscina
by NickM Go to last post
2 829
As the title says, I have been using iontophoresis for over a decade, since early 2005 in fact. I stick to a schedule of treatment once every 3 days to keep my profuse palmer hyperhidrosis at bay. I am weary and tired of this treatment. I need the cure soon, I mean really soon. I'm looking at you miraDry. I need these sweat glands to be destroyed... by sweat2017
by NickM Go to last post
1 835
I think I've established myself on here pretty well. It's time to give up and sell my Fischer unit. It's been sitting around collecting dust for several years now since I began using the Pulsed Current Galvanic Stimulator Comes with the main unit of course and the cables. Trays you can make yourself. I'm asking $150 + whatever priority... by Sprawling
by Sprawling Go to last post
1 633
So I underwent ETS surgery for excessive hand sweating in January of 2017. Let me first say, so far, it has been the best decision of my life! Brief history: I have dealt with excessive hand, feet, and armpit sweat since about the 7th grade. I am currently 27 years old now. To be honest, I was ok with hiding my hand sweat and avoided... by JoeSmith
by JoeSmith Go to last post
6 1,515
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